Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18600 | A08 | 14851014 | C | T | missense_variant | MODERATE | c.263G>A|p.Gly88Asp |
S67 |
2 | BAA08g18600 | A08 | 14851751 | G | A | upstream_gene_variant | MODIFIER | c.-475C>T| |
S191 |
3 | BAA08g18600 | A08 | 14853705 | G | A | upstream_gene_variant | MODIFIER | c.-2429C>T| |
S109 |
4 | BAA08g18600 | A08 | 14854396 | C | T | upstream_gene_variant | MODIFIER | c.-3120G>A| |
S152 |
5 | BAA08g18600 | A08 | 14854762 | G | A | upstream_gene_variant | MODIFIER | c.-3486C>T| |
S257 |